TY  - GEN
AU  - Caimi-Martinez, Fiama
AU  - Antoniutti, Guido
AU  - Blanco, Rocío
AU  - García de la Villa, Bernardo
AU  - Alvarenga, Nelson
AU  - Govea-Callizo, Nancy
AU  - Torres-Juan, Laura
AU  - Heine-Suñer, Damián
AU  - Rosell-Andreo, Jordi
AU  - Crémer Luengos, David
AU  - Álvarez-Rubio, Jorge
AU  - Ripoll-Vera, Tomás
PY  - 2022
DO  - 10.3390/genes13050782
UR  - https://hdl.handle.net/20.500.12105/23486
AB  - Introduction: Arrhythmogenic cardiomyopathy (ACM) is an inherited disease characterized by progressive fibroadipose replacement of cardiomyocytes. Its diagnosis is based on imaging, electrocardiographic, histological and genetic/familial criteria. The...
LA  - eng
PB  - Multidisciplinary Digital Publishing Institute (MDPI)
KW  - Cardiomyopathies
KW  - CVD genetics
KW  - NGS for diagnostics of CVDs-
KW  - Cardiomyopathies
KW  - Heart Diseases
KW  - Humans
KW  - Genetic Association Studies
KW  - Electrocardiography
KW  - Arrhythmias, Cardiac
TI  - New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy
TY  - research article
ER  -